Drug factory · FDA FEI 1940118
Pfizer Inc
875 Chesterfield Parkway W, Chesterfield, MO, United States
No problems found at FDA's last inspection, Aug 20, 2019.
No Action Indicated: inspectors found no objectionable conditions.
4 drug inspections on record since 2012: 3 with no problems, 1 with problems fixed voluntarily, 0 with FDA action.
What it does, for whom
| Drug | Role | For | NDC |
|---|---|---|---|
| Amlodipine and Atorvastatin | Tests it | Pfizer Laboratories Div Pfizer Inc, Prasco Laboratories | 0069-2150, 0069-2160, 0069-2170 +24 |
| Meningococcal Groups A, B, C, W, and Y Vaccine | Makes the active ingredient and tests it | Pfizer Laboratories Div Pfizer Inc | 0069-0600 |
| Pegfilgrastim | Tests it | Pfizer Laboratories Div Pfizer Inc | 0069-0324 |
| Phenytoin | Tests it | Prasco Laboratories | 66993-372 |
| Pneumococcal 20-Valent Conjugate Vaccine | Makes the active ingredient and tests it | Wyeth Pharmaceutical Division of Wyeth Holdings LLC | 0005-2000 |
FDA inspection history
| Ended | Result | Program | Problems noted |
|---|---|---|---|
| Aug 20, 2019 | No problems found | Drug Quality Assurance | — |
| Feb 16, 2016 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| May 21, 2014 | No problems found | Drug Quality Assurance | — |
| Feb 29, 2012 | No problems found | Drug Quality Assurance | — |
Registered with FDA for: analysis; api manufacture.